The original article included "100 mg/ml heparin" to describe the hybridization buffer, but it should correctly read "100 g/ml heparin." The corrected sentence is published in full below. The authors regret this error. "Hybridization buffer: 50% formamide, 0.3 mg/ml yeast RNA (ICN), 100 g/ml hepari
Detection of rhinovirus RNA in middle turbinate of patients with common colds by in situ hybridization
✍ Scribed by Anne Pitkäranta; Tuomo Puhakka; Mika J. Mäkelä; Olli Ruuskanen; Olli Carpen; Antti Vaheri
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 226 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Human rhinovirus 14 RNA was determined by in situ hybridization from middle turbinate biopsies in 32 patients with diagnosed common colds and in five control individuals. Twenty‐two (69%) biopsies from common colds patients but none of the five control biopsies showed reactivity for human rhinovirus 14 antisense probe. The signal was detected both in the respiratory epithelium and in mucosal inflammatory cells. In situ hybridization of the middle turbinate tissue yielded more positive results than RT‐PCR (47%) or virus culture (34%) assayed from nasopharyngeal aspirates, but no statistical significant differences were observed (P = 0.265, P = 0.425, respectively). The results indicated that in situ hybridization procedure was slightly more sensitive than PCR assays and classical culture for the detection of human rhinovirus infection of upper respiratory tract. However, in situ hybridization procedure appeared to be an interesting methodology to investigate the physiopathology of respiratory tract infection by rhinoviruses. J. Med. Virol. 70: 319–323, 2003. © 2003 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract ## BACKGROUND Breast carcinoma and precancer are believed to start in the lining of the milk duct or lobule. Ductography and fiberoptic ductoscopy (FDS) are used to identify abnormal intraductal lesions, although it is difficult to distinguish malignant from benign cases. Therefore, we
## Abstract A rapid technique for the detection of hepatitis C virus (HCV) RNA in liver section using noniso‐topic in situ hybridization was described. Only 3 of the 10 patients seropositive for antibody to HCV and HCV RNA had detectable HCV RNA in the hepatocytes (1%, 2%, and 15% of cells positive
## Methods Mice DBM2 male mice were bred at the Walter and Eliza Hall Institute and were used when aged 6-8 weeks. Antibody The murine IgG2a monoclonal antibody F23.1 (Staerz et al., 1985) was purified from ascites by